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What tags to use when exporting or moving sheep and goats to the EU or Northern Ireland, what to record in your holding register, and how to report the movement.
Find out about group and divisional VAT registration and the forms you should use to apply.
Rules on labelling food, feed and seed as organic or using organic production terms if you produce, prepare, store, import, export or sell organic food in the UK.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
Find codes to use in the Customs Declaration Service (Appendix 13).
Dual citizenship (also known as dual nationality) is allowed in the UK. Read the rules and how to apply.
How growers and traders can get authorised as a professional operator to issue plant passports, when you need to be authorised and plants that need passports.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to use the dual registration measure if you are a specialist events haulier.
Guidance for manufacturers, importers and distributors.
Find out what compound products are, and how to import or move them from the EU to Great Britain.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance providing practical information for placing construction products on the GB market.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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